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Radiobiological Implications of Nanoparticles Following Radiation Treatment
Materials with a high atomic number (Z) are shown to cause an increase in the level of cell kill by ionizing radiation when introduced into tumor cells. This study uses in vitro experiments to investigate the differences in radiosensitization between two cell lines (MCF‐7 and U87) and three commerci...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427468/ https://www.ncbi.nlm.nih.gov/pubmed/34526737 http://dx.doi.org/10.1002/ppsc.201900411 |
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author | Ahmad, Reem Schettino, Giuseppe Royle, Gary Barry, Miriam Pankhurst, Quentin A. Tillement, Olivier Russell, Ben Ricketts, Kate |
author_facet | Ahmad, Reem Schettino, Giuseppe Royle, Gary Barry, Miriam Pankhurst, Quentin A. Tillement, Olivier Russell, Ben Ricketts, Kate |
author_sort | Ahmad, Reem |
collection | PubMed |
description | Materials with a high atomic number (Z) are shown to cause an increase in the level of cell kill by ionizing radiation when introduced into tumor cells. This study uses in vitro experiments to investigate the differences in radiosensitization between two cell lines (MCF‐7 and U87) and three commercially available nanoparticles (gold, gadolinium, and iron oxide) irradiated by 6 MV X‐rays. To assess cell survival, clonogenic assays are carried out for all variables considered, with a concentration of 0.5 mg mL(−1) for each nanoparticle material used. This study demonstrates differences in cell survival between nanoparticles and cell line. U87 shows the greatest enhancement with gadolinium nanoparticles (2.02 ± 0.36), whereas MCF‐7 cells have higher enhancement with gold nanoparticles (1.74 ± 0.08). Mass spectrometry, however, shows highest elemental uptake with iron oxide and U87 cells with 4.95 ± 0.82 pg of iron oxide per cell. A complex relationship between cellular elemental uptake is demonstrated, highlighting an inverse correlation with the enhancement, but a positive relation with DNA damage when comparing the same nanoparticle between the two cell lines. |
format | Online Article Text |
id | pubmed-8427468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84274682021-09-13 Radiobiological Implications of Nanoparticles Following Radiation Treatment Ahmad, Reem Schettino, Giuseppe Royle, Gary Barry, Miriam Pankhurst, Quentin A. Tillement, Olivier Russell, Ben Ricketts, Kate Part Part Syst Charact Full Papers Materials with a high atomic number (Z) are shown to cause an increase in the level of cell kill by ionizing radiation when introduced into tumor cells. This study uses in vitro experiments to investigate the differences in radiosensitization between two cell lines (MCF‐7 and U87) and three commercially available nanoparticles (gold, gadolinium, and iron oxide) irradiated by 6 MV X‐rays. To assess cell survival, clonogenic assays are carried out for all variables considered, with a concentration of 0.5 mg mL(−1) for each nanoparticle material used. This study demonstrates differences in cell survival between nanoparticles and cell line. U87 shows the greatest enhancement with gadolinium nanoparticles (2.02 ± 0.36), whereas MCF‐7 cells have higher enhancement with gold nanoparticles (1.74 ± 0.08). Mass spectrometry, however, shows highest elemental uptake with iron oxide and U87 cells with 4.95 ± 0.82 pg of iron oxide per cell. A complex relationship between cellular elemental uptake is demonstrated, highlighting an inverse correlation with the enhancement, but a positive relation with DNA damage when comparing the same nanoparticle between the two cell lines. John Wiley and Sons Inc. 2020-03-03 2020-04 /pmc/articles/PMC8427468/ /pubmed/34526737 http://dx.doi.org/10.1002/ppsc.201900411 Text en © 2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Ahmad, Reem Schettino, Giuseppe Royle, Gary Barry, Miriam Pankhurst, Quentin A. Tillement, Olivier Russell, Ben Ricketts, Kate Radiobiological Implications of Nanoparticles Following Radiation Treatment |
title | Radiobiological Implications of Nanoparticles Following Radiation Treatment |
title_full | Radiobiological Implications of Nanoparticles Following Radiation Treatment |
title_fullStr | Radiobiological Implications of Nanoparticles Following Radiation Treatment |
title_full_unstemmed | Radiobiological Implications of Nanoparticles Following Radiation Treatment |
title_short | Radiobiological Implications of Nanoparticles Following Radiation Treatment |
title_sort | radiobiological implications of nanoparticles following radiation treatment |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427468/ https://www.ncbi.nlm.nih.gov/pubmed/34526737 http://dx.doi.org/10.1002/ppsc.201900411 |
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